SNP Report

Basic Info

Name	rs38495 dbSNP Ensembl
Location	chr7:30586661 - 30586661(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.357029
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000426529, ENST00000578994, ENST00000579174, ENST00000580440, ENST00000581665, ENST00000581794, ENST00000582549, ENST00000582733, ENST00000583664, ENST00000584199, ENST00000584372); non_coding_transcript_variant(ENST00000426529, ENST00000578994, ENST00000579174, ENST00000580440, ENST00000581665, ENST00000581794, ENST00000582549, ENST00000582733, ENST00000583664, ENST00000584199, ENST00000584372); upstream_gene_variant(ENST00000454922)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 0)

SNPs in LD with rs38495 (count: 0) View in gBrowse (chr7:30586661..30586661 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)